3. Mutations in the GHR Gene
3.1. GLU44LYS, rs121909361
One of the mutations that was diagnosed by Goddard et al.
[21][8] was a mutation located in exon 4 that introduced lysine instead of glutamic acid at position 44 (Glu44Lys) in 184 base pairs
(Figure 2). The mutation in this exon was inherited from the father. The authors of the study analyzed the effect of this mutation on the GH-binding ability of GHR. The Glu44 residue is in direct contact with the GH, and the introduction of lysine at position 44 reduced the binding by 330, compared to the wild-type receptor binding. It was therefore found that this mutation is responsible for a decreased affinity for GH.
3.2. ARG161CYS, rs121909362
Another mutation that was reported by Goddard et al.
[21][8] was a mutation in exon 6, at 535 base pairs (
Figure 21). It introduced a cysteine at position 161 (Arg161Cys) in place of arginine. The cysteine in this mutation was potentially misfolded. The mutation was inherited from the mother’s side. One of the patients studied by Goddard was heterozygously composed of the Glu44Lys and Arg161Cys mutations, and he was more affected by partial GH sensitivity than his homozygous parents (father had the Glu44Lys mutation, mother had Arg161Cys). Similar to the rest of the study participants, he was treated with GH, but the response to this treatment was poor, and so it was concluded that the reason for this may be mutations that cause partial sensitivity to GH due to dysfunctional GHRs.
3.3. GLU224ASP, rs45588036
The last mutation discovered by Goddard et al.
[21][8] was found in exon 7 (
Figure 21), and it was a mutation in the 726 base pair that introduced aspartic acid in place of glutamic acid at position 224 (Glu224Asp). However, the conservative substitution in this mutation was expressed at normal expression levels and resembled the mutant Arg211His protein, so that the GH affinity for the
GHR gene that contains the Glu224Asp mutation was nearly normal. A possible effect of this mutation was incorrect subcellular localization. Partial GH insensitivity, which can be manifested by short stature, may occur in individuals who have heterozygous mutations in the
GHR gene due to mutations in other genes, or when changes confer a dominant phenotype. Patients were selected, in part, on the basis of decreased serum GHBP levels, which suggest that the mutations discussed by Goddard may directly affect ligand binding. In the case of the Glu44Lys mutation, a 330-fold decrease in the affinity of the GH receptor to GHBP was observed, while the remaining mutations had smaller effects on the ligand binding.
3.4. IVS8AS, G-C, -1 rs730880308
Ayling et al.
[28][15] report the case of a family in which a GHIS causal mutation, IVS8AS, was recognized in the mother and daughter, which was located in the cytoplasmic domain of the GH receptor, which is an inherited domain. It was a single heterozygous mutation that transverses G to C at position 1 of the 3′ splicing acceptor site that precedes exon 9 of the
GHR (
Figure 21). The fusion of JAK2 with the GHR requires a conserved exon 9-encoded sequence that is located in the cytoplasmic domain. This mutation had a dominant negative effect, which caused a shortening of the cytoplasmic part of the protein, and it was associated with GHBP. Most of the previously discovered
GHR mutations were located in the extracellular binding domain of the GHR. However, in the study, Ayling indicates that dominant
GHR mutations should be looked for in children with normal GHBP levels and low body heights; that is, in children with no previous suspected endocrinopathy.
3.5. VAL144ILE, rs6413484
A study by Sanchez et al.
[13][16] discovered the last known mutation in the growth hormone receptor gene so far, which was the VAL144ILE mutation, which is located on exon 6. It was found in one subject with a short body height and in two members of her family, who also had shorter body heights (
Figure 21). A study by Amslem et al.
[20][7] describes the same amino acid that is changed in this family. The significance of this mutation has not been fully established; however, it seems likely that this mutation affects height. The potential significance of this mutation was established from the above-described work by Ayling et al.
[28][15], in which the patient with GHIS had a mutated allele on the same amino acid (144) as the patient in the study by Sanchez et al.
[13][16]. However, this mutation occurred in a different base pair. This change was related to GHIS, and so the amino acid V144 was found to be important for the GH receptor function.
4. Mutations in the IGF1R Gene
4.1 ARG108GLN, rs121912426
Abuzzahab et al.
[24] [11], after examining 51 people who showed short postnatal growth, found a mutation in the
IGF1R IGF1R gene in two of them. Both of these mutations were found in exon 2 (
Figure 3Figure 2). The first person described had two mutations. The first was a single base pair substitution at the codon of amino acid 108 that changed arginine into glutamine. The mutation at position 108, ARG108GLN, was inherited from the father. This mutation affected the α and β cleavage site, which resulted in the intracellular sequestration of the unprocessed proreceptor, and decreased
IGF1R IGF1R expression
[32][17].
4.2 LYS115ASN, rs121912427
The second mutation described by Abuzzahab et al. [24] in the first of 51 patients was a mutation in IGF1R that consisted of replacing lysine with asparagine at amino acid codon 115 (
Figure 32). This mutation, LYS115ASN, was inherited from the mother. In the person who had these mutations, each of the α subunits in the mature receptor contained one of these mutations in various combinations, which is due to the heterotetrameric structure of IGF1R. These mutations changed the conformation of the IGF1R-binding domain and, consequently, reduced ligand binding. The binding of IGF-1 to IGF1R on the fibroblasts in the patient was reduced by one-third compared to the control group. Receptor phosphory-lation in response to IGF-1 was also investigated to determine decreased hormone binding to receptor signaling. Phosphorylation was dose-dependent in fibroblasts; however, it showed a decrease in sensitivity compared to the control group. The subject was treated with growth hormone, during which the concentration of IGF-1 in the serum increased, which indicated abnormal GH secretion.
4.3 ARG59TER, rs121912428
Abuzzahab et al.
[24][11] also found mutations in a patient who showed a low body height and a slow growth rate. This patient was heterozygous for the early transcriptional termination mutation at exon 2 at position 59, which should contain arginine (
Figure 32). This mutation was inherited from the mother, who was also born SGA. This mutation inactivates one
IGF1R IGF1R allele, and the protein may not be expressed; however, if expressed, it would only correspond to the N-terminal end of the
IGF1R IGF1R α chain, and the receptor would not be able to bind IGF-1. It was suggested that individuals with the ARG59TER mutation may exhibit a haploinsufficiency phenotype, as the biallelic expression of wild
-type and mutant
IGF1R IGF1R alleles was detected in the blood of the patient. After examining the phosphorylation of Akt, the
IGF1R IGF1R signaling protein, and following an analysis of the post-receptor signal transduction, it was proposed that the IGF-1 resistance in the subject was due to a reduced number of IGF1R
[32][17].
4.4 ARG709GLN, rs121012429
The ARG709GLN mutation was discovered by Kawashima et al.
[29][18]. They examined 24 people who were characterized by low body heights and IUGR. One person was identified with a mutation in the
IGF1R IGF1R gene that was heterozygous for arginine to glutamine conversion at position 709 (
Figure 32). This mutation was inherited from the mother and it changed the IGF1R proreceptor cleavage site by losing the restriction site. ARG709GLN affected the cleavage site between the α and β subunits, which caused the intracellular sequestration of the unprocessed proreceptor, and the decreased expression of fully digested and processed IGF1R
[32][17].
4.5 ARG481GLN, rs33958176
In another study, Inagaki et al.
[30][19] describes a mutation that was found in a girl with a short body height. This mutation was based on the replacement of arginine with glutamine at position 481 of exon 7
IGF1R IGF1R (
Figure 32). This mutation was inherited from the maternal side. Researchers observed an increase in tyrosine phosphorylation after IGF-1 stimulation in the mutant
IGF1R, IGF1R, compared to wild-type, and decreases in Akt phosphorylation and in proliferation in cells that overexpressed mutant
IGF1R IGF1R. Because of the mutation site being close to the first of the four disulfide bonds that connect the α and β subunits, it was suggested that this mutation disrupted this binding and resulted in incomplete dimerization and conformational alteration.
4.6 GLU121LYS, rs15554342084.6. GLU121LYS, rs1555434208
The GLU121LYS and GLU234LYS mutations were discovered and described in the study by Fang et al.
[31][20]. Two siblings were examined, one of whom had IUGR, and the other who had a short body height. Subjects had complex heterozygous missense mutations in the
IGF1R IGF1R gene. One was found in exon 2 and consisted of replacing glutamic acid with lysine at position 121 (
Figure 32). This mutation was also found in the mother of the studied siblings.
4.7 GLU234LYS, rs12531038064.7. GLU234LYS, rs1253103806
The second mutation reported by Fang et al.
[31][20] is the mutation that is involved in replacing glutamic acid with lysine at position 234 of exon 2 (
Figure 32). This mutation was inherited from the father of the subjects. These mutations resulted in decreased expression of mature and functional IGF1R peptides, with a consequently decreased activation of the IGF1R pathway in response to IGF-1. Analysis of sibling fibroblasts showed an 80% reduction in processed α and β subunits, compared to wild-type receptors.
4.8 ARG10LEU, rs14090587834.8. ARG10LEU, rs1409058783
The penultimate mutation identified so far in the
IGF1R IGF1R gene was discovered and described by Gannage-Yared et al.
[25][12]. They examined a patient born with IUGR who exhibited low body height later in life. A missense mutation in exon 2 was identified to convert arginine to leucine at position 10 (
Figure 32). This mutation was inherited from both parents, who were its heterozygous carriers. This mutation resulted in the loss of hydrogen bonds between Leu10 and Asp8 in the
IGF1R IGF1R. The total expression of
IGF1R IGF1R containing this mutation was unchanged; however, impaired IGF receptor activation and decreased IGF1R autophosphorylation were observed in the subject’s fibroblasts, and greater amounts of IGF-1 were required to achieve a similar level of Akt phosphorylation as in the controls with receptors without this mutation.
4.9 EX10, rs1555460945, c.2201G-T4.9. EX10, rs1555460945, c.2201G-T
The most recent mutation in the
IGF1R IGF1R gene to date is reported by Prontera et al.
[26][13]. The mutation carrier was a patient born with IUGR. The mutation in this person consisted of a c.2201G-T transversion that was identified on the last nucleotide in exon 10 (
Figure 32). The examined person showed reduced autophosphorylation in fibroblasts and lower Akt activity, and an abnormal isoform that generates a mutant protein that contains 25 additional amino acids. The studies carried out by the authors of the study indicate the impaired ability of the
IGF1R IGF1R that contains this mutation to self-phosphorylate and to activate the downstream IGF-1 signaling pathway and the insulin–Akt complex.